| manager |
|
| language |
- |
| license |
- |
| created at |
2021-12-22 03:08:20 UTC |
| updated at |
2021-12-22 07:06:09 UTC |
|
MONDO_bioport_pref_name
|
183,974 entries
|
There is 0 pattern entry.
|
deficiency syndromes, immunological
|
3778 |
|
|
capillary hemangioma, lobular
|
D017789 |
|
|
gelsolin type lattice corneal dystrophy
|
C000657784 |
|
|
type 2b loeys-dietz syndrome
|
C537783 |
|
|
type II lattice corneal dystrophy
|
C000657784 |
|
|
corneal dystrophy, lattice type II
|
C000657784 |
|
|
plasmodium falciparum malaria
|
D016778 |
|
|
retinitis pigmentosa, juvenile, aipl1-related
|
C565778 |
|
|
aphalangia syndactyly microcephaly
|
C537787 |
|
|
susceptibility to malignant hyperthermia 1
|
7783 |
|
|
macrocephaly with multiple epiphyseal dysplasia and distinctive facies
|
11778 |
|
|
dermoid cyst of skin
|
1778 |
|
|
papular epidermal nevi with skyline basal cell layers syndrome
|
17785 |
|
|
Hodgkin lymphoma nodular LP, NOS
|
44778 |
|
|
Hodgkin lymphoma nodular lymphocyte predominant type, NOS
|
44778 |
|
